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FDA 510(k)

VALLEY FORGE BIPLOAR LOOP

K-Number: K955764 · 1996-03-01

ApplicantValley Forge Scientific Corp.
Decision Date1996-03-01
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VALLEY FORGE BIPLOAR LOOP is the device name listed in this FDA 510(k) record. The listed applicant is Valley Forge Scientific Corp.. It received FDA 510(k) clearance on 1996-03-01 under 510(k) number K955764. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALLEY FORGE BIPLOAR LOOP?

VALLEY FORGE BIPLOAR LOOP is a medical device that received FDA 510(k) clearance on 1996-03-01. The listed applicant is Valley Forge Scientific Corp.. The 510(k) number is K955764.

When did VALLEY FORGE BIPLOAR LOOP receive FDA 510(k) clearance?

VALLEY FORGE BIPLOAR LOOP received FDA 510(k) clearance on 1996-03-01, under 510(k) number K955764.

Who is the listed applicant for VALLEY FORGE BIPLOAR LOOP?

The FDA 510(k) record lists Valley Forge Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VALLEY FORGE BIPLOAR LOOP?

The FDA product code for VALLEY FORGE BIPLOAR LOOP is GEI.

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Other records listing Valley Forge Scientific Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K050364MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEMK042604VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL INSTRUMENTSK032601STRYKER INTERVENTIONAL PAIN RF GENERATORK033499MALIS IRRIGATION MODULE 1000K982229BI-DENTK973554VALLEY FORGE BIPOLAR BALL TIP ELECTRODE

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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